Henry's Law Constants

Rolf Sander

Atmospheric Chemistry Division

Max-Planck Institute for Chemistry
Mainz, Germany

Errata

Contact, Imprint, Acknowledgements

When referring to the compilation of Henry's Law Constants, please cite this publication:

R. Sander: Compilation of Henry's law constants (version 5.0.0) for water as solvent, Atmos. Chem. Phys., 23, 10901-12440 (2023), doi:10.5194/acp-23-10901-2023

The publication from 2023 replaces that from 2015, which is now obsolete. Please do not cite the old paper anymore.

Henry's Law Constants → Organic species with chlorine (Cl) → Chlorocarbons (C, H, Cl) → α-1,2,3,4,5,6-hexachlorocyclohexane

FORMULA:	C₆H₆Cl₆
TRIVIAL NAME:	α-lindane; α-HCH
CAS RN:	319-84-6
STRUCTURE (FROM NIST):
InChIKey:	JLYXXMFPNIAWKQ-SHFUYGGZSA-N

$H_{s}^{cp}$	$d ln H_{s}^{cp} / d (1/ T)$	References	Type	Notes
[mol/(m³Pa)]	[K]
1.5		Xiao et al. (2004)	L	368)
1.4		Xiao et al. (2004)	L	369)
3.0	5500	Cetin et al. (2006)	M
1.7	7500	Sahsuvar et al. (2003)	M
8.1×10⁻¹		Altschuh et al. (1999)	M
1.3	6500	Kucklick et al. (1991)	M
4.2×10⁻¹		Atlas et al. (1982)	M	681)
1.1		Mackay et al. (2006d)	V
9.1×10⁻¹		Ballschmiter and Wittlinger (1991)	V
2.3		Calamari et al. (1991)	V	12)
1.1		Suntio et al. (1988)	V	12)
5.9×10⁻³	3900	Paasivirta et al. (1999)	T
1.8		Suntio et al. (1988)	C	682)
3.9×10⁻²		Zhang et al. (2010)	Q	288) 289)
7.7		Zhang et al. (2010)	Q	288) 290)
4.0×10¹		Zhang et al. (2010)	Q	288) 291)
3.8×10⁻¹		Zhang et al. (2010)	Q	288) 292)
1.1		Modarresi et al. (2007)	Q	68)
	7100	Kühne et al. (2005)	Q
	7100	Kühne et al. (2005)	?

Data

The first column contains Henry's law solubility constant

H_{s}^{cp}

at the reference temperature of 298.15 K.
The second column contains the temperature dependence

d ln H_{s}^{cp} / d
(1/ T)

, also at the reference temperature.

References

Altschuh, J., Brüggemann, R., Santl, H., Eichinger, G., & Piringer, O. G.: Henry’s law constants for a diverse set of organic chemicals: Experimental determination and comparison of estimation methods, Chemosphere, 39, 1871–1887, doi:10.1016/S0045-6535(99)00082-X (1999).
Atlas, E., Foster, R., & Giam, C. S.: Air-sea exchange of high-molecular weight organic pollutants: laboratory studies, Environ. Sci. Technol., 16, 283–286, doi:10.1021/ES00099A010 (1982).
Ballschmiter, K. & Wittlinger, R.: Interhemisphere exchange of hexachlorocyclohexanes, hexachlorobenzene, polychlorobiphenyls, and 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane in the lower troposphere, Environ. Sci. Technol., 25, 1103–1111, doi:10.1021/ES00018A014 (1991).
Calamari, D., Bacci, E., Focardi, S., Gaggi, C., Morosini, M., & Vighi, M.: Role of plant biomass in the global environmental partitioning of chlorinated hydrocarbons, Environ. Sci. Technol., 25, 1489–1495, doi:10.1021/ES00020A020 (1991).
Cetin, B., Ozer, S., Sofuoglu, A., & Odabasi, M.: Determination of Henry’s law constants of organochlorine pesticides in deionized and saline water as a function of temperature, Atmos. Environ., 40, 4538–4546, doi:10.1016/J.ATMOSENV.2006.04.009 (2006).
Kucklick, J. R., Hinckley, D. A., & Bidleman, T. F.: Determination of Henry’s law constants for hexachlorocyclohexanes in distilled water and artificial seawater as a function of temperature, Mar. Chem., 34, 197–209, doi:10.1016/0304-4203(91)90003-F (1991).
Kühne, R., Ebert, R.-U., & Schüürmann, G.: Prediction of the temperature dependency of Henry’s law constant from chemical structure, Environ. Sci. Technol., 39, 6705–6711, doi:10.1021/ES050527H (2005).
Mackay, D., Shiu, W. Y., Ma, K. C., & Lee, S. C.: Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, vol. IV of Nitrogen and Sulfur Containing Compounds and Pesticides, CRC/Taylor & Francis Group, doi:10.1201/9781420044393 (2006d).
Modarresi, H., Modarress, H., & Dearden, J. C.: QSPR model of Henry’s law constant for a diverse set of organic chemicals based on genetic algorithm-radial basis function network approach, Chemosphere, 66, 2067–2076, doi:10.1016/J.CHEMOSPHERE.2006.09.049 (2007).
Paasivirta, J., Sinkkonen, S., Mikkelson, P., Rantio, T., & Wania, F.: Estimation of vapor pressures, solubilities and Henry’s law constants of selected persistent organic pollutants as functions of temperature, Chemosphere, 39, 811–832, doi:10.1016/S0045-6535(99)00016-8 (1999).
Sahsuvar, L., Helm, P. A., Jantunen, L. M., & Bidleman, T. F.: Henry’s law constants for α-, β-, and γ-hexachlorocyclohexanes (HCHs) as a function of temperature and revised estimates of gas exchange in Arctic regions, Atmos. Environ., 37, 983–992, doi:10.1016/S1352-2310(02)00936-6 (2003).
Suntio, L. R., Shiu, W. Y., Mackay, D., Seiber, J. N., & Glotfelty, D.: Critical review of Henry’s law constants for pesticides, Rev. Environ. Contam. Toxicol., 103, 1–59, doi:10.1007/978-1-4612-3850-8_1 (1988).
Xiao, H., Li, N., & Wania, F.: Compilation, evaluation, and selection of physical-chemical property data for α-, β-, and γ-hexachlorocyclohexane, J. Chem. Eng. Data, 49, 173–185, doi:10.1021/JE034214I (2004).
Zhang, X., Brown, T. N., Wania, F., Heimstad, E. S., & Goss, K.-U.: Assessment of chemical screening outcomes based on different partitioning property estimation methods, Environ. Int., 36, 514–520, doi:10.1016/J.ENVINT.2010.03.010 (2010).

Type

Table entries are sorted according to reliability of the data, listing the most reliable type first: L) literature review, M) measured, V) VP/AS = vapor pressure/aqueous solubility, R) recalculation, T) thermodynamical calculation, X) original paper not available, C) citation, Q) QSPR, E) estimate, ?) unknown, W) wrong. See Section 3.1 of Sander (2023) for further details.

Notes

12)	Value at T = 293 K.
68)	Modarresi et al. (2007) use different descriptors for their calculations. They conclude that a genetic algorithm/radial basis function network (GA/RBFN) is the best QSPR model. Only these results are shown here.
288)	Data taken from the supplement.
289)	Calculated using the EPI Suite (v4.0) method.
290)	Calculated using the SPARC (v4.2) method.
291)	Calculated using the COSMOtherm (v2.1) method.
292)	Calculated using the ABSOLV (ADMEBoxes v4.1) method.
368)	Literature-derived value.
369)	Final adjusted value.
681)	As explained by Miller and Stuart (2003), the measurements were performed at 296 K.
682)	Value for T = 295... 298 K.

The numbers of the notes are the same as in Sander (2023). References cited in the notes can be found here.

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